Abstract
Humulus yunnanensis is an endemic species in Yunnan, China, which is used for beer and pharmacology industry. The phylogenetic position of this species in Humulus remains controversial. The complete chloroplast (cp) genome sequence of H. yunnanensis was reported and characterized in this study. The cp genome is 153,612 bp in length and contains a pair of inverted repeats (IRs, 29,824 bp) separated by a large (87,728 bp) and small (15,390 bp) single-copy regions. A total of 112 unique genes were predicted, including 78 protein-coding genes, 30 tRNA genes, and 4 rRNA genes. The phylogenetic analysis revealed that H. yunnanensis is more closely related to H. scandens than H. lupulus.
Keywords: Chloroplast genome, Humulus yunnanensis, Humulus, phylogenetic analysis
Humulus is a small genus of Cannabaceae native to temperate regions of Northern Hemisphere. Three recognized species, H. lupulus, H. scandens, and H. yunnanensis are widely used in brewing, medicinal, and pharmaceutical industries. However, the phylogenetic relationships within Humulus have been questioned (Yang et al. 2013; Boutain 2014). Yang’s molecular phylogenetic study based on four plastid loci (atpB-rbcL, rbcL, rps16, and trnL-trnF) indicated that H. yunnanensis and H. lupulus consisted of the sister group (Yang et al. 2013). However, based on the phylogenetic result from nuclear ribosomal DNA (ITS2) and cpDNA (petL-psbE), Boutain (2014) validated that H. yunnanensis shared a closer evolutionary history with H. scandens than H. lupulus. To further determine the phylogenetic placement of H. yunnanensis, we sequenced the complete chloroplast (cp) genome of H. yunnanensis using high-throughput sequencing technology.
The fresh leaf of H. yunnanensis was collected from Kunming (Yunnan, Southwest of China). Specimens (14CS9673) were deposited in the herbarium of the Kunming Institute of Botany, CAS (KUN). Total genomic DNA was extracted with a modified CTAB method (Doyle and Doyle 1987). Illumina paired-end library was constructed and sequenced using the Illumina HiSeq 2500 (Illumina, CA, USA) at Novogene (Beijing, China). Approximately, 2 Gb raw data were generated. The assembly of the complete cp genome was accomplished using SPAdes (Bankevich et al. 2012). All genes encoding proteins, transfer RNAs (tRNAs), and ribosomal RNAs (rRNAs) were automatically annotated using Dual Organellar Genome Annotator (DOGMA) (Wyman et al. 2004) coupled with manual corrections.
The complete cp genome of H. yunnanensis (GenBank accession number: MK423880) is 153,612 bp in length and has a typical quadripartite structure. It comprises a large single-copy region (LSC, 83,697 bp) and a small single-copy region (SSC, 17,677 bp) separated by a pair of inverted repeats (IRs, 26,119 bp each). The overall GC content of the cp genome is 36.9%, while that of IRs (42.5%) is higher than that of LSC (34.6%) and SSC (30.8%) regions. The H. yunnanensis cp genome encodes 112 unique genes including 78 protein-coding genes, 30 tRNA, and 4 rRNA genes. There are 19 intron-containing genes, in which 10 protein-coding (rps16, rpl16, rpl2, rps12, rpoC1, ndhA, ndhB, petB, petD, and atpF) and 6 tRNA (trnA-UGC, trnG-UCC, trnI-GAU, trnK-UUU, trnL-UAA, and trnV-UAC) genes has a single intron and 3 genes (clpP, rps12, and ycf3) has two introns.
In this study, the phylogenetic analysis was performed with the newly sequenced cp genome of H. yunnanensis and two previously released cp genomes of H. scandens and H. lupulus. Eleven species of other five genera in Cannabaceae were used as outgroups. The identical maximum likelihood (ML) and Bayesian phylogenetic trees indicated that three species from the genus Humulus formed a monophyletic clade with 100% bootstrap and 1.0 posterior probability support, respectively (Figure 1). Moreover, H. yunnanensis was supported more closely related to H. scandens than H. lupulus (Figure 1).
Figure 1.
The maximum likelihood (ML) tree of Humulus inferred from the complete chloroplast genome sequences. Numbers at nodes correspond to ML bootstrap percentages (1,000 replicates) and Bayesian inference (BI) posterior probabilities.
Disclosure statement
No potential conflict of interest was reported by the authors.
References
- Bankevich A, Nurk S, Antipov D, Gurevich AA, Dvorkin M, Kulikov AS, Lesin VM, Nikolenko SI, Pham S, Prjibelski AD, et al. 2012. Spades: A new genome assembly algorithm and its applications to single-cell sequencing. J Comput Biol. 19:455–477. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Boutain JR. 2014. On the origin of hops: genetic variability, phylogenetic relationships, and ecological plasticity of Humulus (Cannabaceae) [Dissertations] Hawaii: University of Hawaii at Manoa. [Google Scholar]
- Doyle JJ, Doyle JL. 1987. A rapid DNA isolation procedure for small quantities of fresh leaf tissue. Phytochem Bull. 19:11–15. [Google Scholar]
- Wyman SK, Jansen RK, Boore JL. 2004. Automatic annotation of organellar genomes with DOGMA. Bioinformatics. 20:3252–3255. [DOI] [PubMed] [Google Scholar]
- Yang MQ, van Velzen R, Bakker FT, Sattarian A, Li DZ, Yi TS. 2013. Molecular phylogenetics and character evolution of Cannabaceae. Taxon. 62:473–485. [Google Scholar]